| Diseases |
Alias |
|
| Hypothyroidism, Congenital, Nongoitrous, 5 |
|
CHNG5
|
Hypothyroidism, Congenital Nongoitrous, 5
|
|
Congenital Nongoitrous Hypothyroidism 5
|
Hypothyroidism, Congenital, Non-Goitrous, 5
|
|
Hypothyroidism, Congenital, Nongoitrous, Type 5
|
|
|
| Ventricular Septal Defect 3 |
|
|
| Atrial Septal Defect 7 With Or Without Atrioventricular Conduction Defects |
|
Asd With Or Without Atrioventricular Conduction Defects
|
ASD7
|
|
Atrial Septal Defect 7, With Or Without Av Conduction Defects
|
Atrial Septal Defect 7, With Or Without Atrioventricular Conduction Defects
|
|
Asd With Atrioventricular Conduction Defects
|
Atrial Septal Defect 7 With Or Without Av Conduction Defects
|
|
Septal Defect, Atrial, Type 7 With/Without Atrioventricular Conduction Defects
|
|
|
| Hypoplastic Left Heart Syndrome 2 |
|
HLHS2
|
Heart, Hypoplastic Left, Syndrome, Type 2
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Atrial Heart Septal Defect 7 |
|
Atrial Septal Defect-Atrioventricular Conduction Defects Syndrome
|
Asd With Or Without Atrioventricular Conduction Defects
|
|
Atrial Septal Defect 7, With Or Without Av Conduction Defects
|
Atrial Septal Defect With Atrioventricular Conduction Defects
|
|
|
| Conotruncal Heart Malformations |
|
Persistent Truncus Arteriosus
|
Conotruncal Anomaly Face Syndrome
|
|
Truncus Arteriosus
|
Common Arterial Trunk
|
|
CTHM
|
Conotruncal Heart Malformations, Variable
|
|
Tac
|
Truncus Arteriosus Communis
|
|
Conotruncal Cardiac Defects
|
Common Aorticopulmonary Trunk
|
|
Cafs
|
Conotruncal Heart Defects
|
|
Cthd
|
Dorv
|
|
Double-Outlet Right Ventricle
|
Pta
|
|
Heart Malformations, Conotruncal
|
Common Truncus
|
|
Common Truncus Arteriosus
|
Persistent Truncus Arteriosus Or Communis
|
|
Truncus Communis
|
Common Aortico-Pulmonary Trunk
|
|
Truncus Arteriosus With Aortic Dominance
|
Truncus Arteriosus With No Aortic Obstruction
|
|
Truncus Arteriosus With Pulmonary Dominance And Interrupted Aortic Arch
|
Truncus Arteriosus With Interrupted Aortic Arch
|
|
Common Arterial Trunk With Interrupted Aortic Arch
|
Van Praagh Truncus Arteriosus Type A4
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Double Outlet Right Ventricle |
|
Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect
|
Taussig-Bing Syndrome
|
|
Dextrotransposition Of Aorta
|
Taussig-Bing Syndrome Or Defect
|
|
Dorv
|
Dorv With Subpulmonary Vsd
|
|
Dorv-Tga
|
Double Outlet Right Ventricle With Transposition Of The Great Arteries
|
|
Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type
|
Taussig-Bing Heart
|
|
Taussig-Bing Malformation
|
Taussig-Bing Complex
|
|
Taussig-Bing Defect
|
Taussig-Bing
|
|
Double Outlet Right Ventricle With Remote Ventricular Septal Defect
|
Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect
|
|
Double Outlet Right Ventricle With Non-Committed Interventricular Communication
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis
|
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Aortic Arch Interruption |
|
Interrupted Aortic Arch
|
Aorta Atresia
|
|
Iaa - [Interrupted Aortic Arch]
|
Aorta Arch Atresia
|
|
Aorta Ring Atresia
|
Aortic Arch Atresia
|
|
Aortic Ring Atresia
|
|
|
| Thyroid Ectopia |
|
|
| Athyreosis |
|
|
| Asplenia, Isolated Congenital |
|
ICAS
|
Splenic Hypoplasia
|
|
Familial Isolated Congenital Asplenia
|
Hyposplenia, Isolated Congenital
|
|
Asplenia, Familial
|
Isolated Congenital Asplenia
|
|
Congenital Hypoplasia Of Spleen
|
Hypoplasia Of Spleen
|
|
Spenlic Hypoplasia
|
Congenital Isolated Hyposplenia
|
|
Familial Asplenia
|
|
|
| Interatrial Communication |
|
Asd
|
Atrial Septal Defect
|
|
Interauricular Communication
|
|
|
| Left Ventricular Noncompaction |
|
Noncompaction Cardiomyopathy
|
Left Ventricular Hypertrabeculation
|
|
Lvnc
|
Spongy Myocardium
|
|
Isolated Noncompaction Of The Ventricular Myocardium
|
Left Ventricular Myocardial Noncompaction Cardiomyopathy
|
|
Fetal Myocardium
|
Honeycomb Myocardium
|
|
Hypertrabeculation Syndrome
|
Left Ventricular Non-Compaction
|
|
Lvht
|
Non-Compaction Of The Left Ventricular Myocardium
|
|
Ventricular Noncompaction, Left
|
Non-Compaction Cardiomyopathy
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| Aortic Valve Disease 1 |
|
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
|
Aortic Valve Disorder
|
AOVD1
|
|
Bav
|
Bicuspid Aortic Valve Disease
|
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
|
Aovd
|
Aortic Valve, Bicuspid
|
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
|
Familial Bav
|
Calcific Aortic Stenosis
|
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
|
Bicommissural Aortic Valve
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
| Hypoplastic Left Heart Syndrome |
|
Hlhs
|
Heart, Hypoplastic Left, Syndrome
|
|
Hypoplasia Of The Left Heart
|
Left Heart Hypoplasia Syndrome
|
|
Hlhs - [Hypoplastic Left Heart Syndrome]
|
Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome
|
|
Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle
|
|
Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia
|
Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome
|
|
Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome
|
|
|
| Deletion 5q35 |
|
Del (5)(Q35)
|
Del (5)(Qter)
|
|
Distal 5q Deletion
|
Monosomy 5q35
|
|
Telomeric Deletion 5q
|
Chromosome 5, Monosomy 5q35
|
|
|
| Heart Septal Defect |
|
Septal Defect
|
Heart Septal Defects
|
|
Cardiac Septal Defects
|
Congenital Septal Defect Of Heart
|
|
|
| Atrioventricular Block |
|
|
| Ventricular Septal Defect |
|
Ventricular Septal Defects
|
Interventricular Septal Defect
|
|
Heart Septal Defects, Ventricular
|
Ventricular Septal Abnormality
|
|
Interventricular Septum Defect
|
Ventricular Septum Defect
|
|
Vsd - [Ventricular Septum Defect]
|
Congenital Ventricular Septal Defect
|
|
Single Ventricular Septal Defect
|
|
|
| Familial Progressive Cardiac Conduction Defect |
|
Familial Lenegre Disease
|
Familial Lev Disease
|
|
Familial Lev-Lenegre Disease
|
Familial Pccd
|
|
Familial Progressive Heart Block
|
Hereditary Bundle Branch Defect
|
|
Hereditary Bundle Branch System Defect
|
|
|
| Ebstein Anomaly |
|
Ebstein'S Anomaly
|
Ebstein'S Anomaly Of Common Atrioventricular Valve
|
|
Ebstein'S Anomaly Of Right Atrioventricular Valve
|
Ebstein'S Anomaly Of Tricuspid Valve
|
|
Ebstein'S Malformation
|
Ebstein Malformation Of The Tricuspid Valve
|
|
Ebstein Anomaly Of The Tricuspid Valve
|
Ebstein Disease
|
|
Accessory Tricuspid Valve Tissue
|
Congenital Ebstein Deformity Of Tricuspid Valve
|
|
Ebstein Syndrome
|
Ebstein Cardiopathy
|
|
Ebstein Anomaly Of Tricuspid Valve
|
|
|
| Holt-Oram Syndrome |
|
HOS
|
Atriodigital Dysplasia
|
|
Heart-Hand Syndrome
|
Atrio-Digital Syndrome
|
|
Cardiac-Limb Syndrome
|
Heart-Hand Syndrome, Type 1
|
|
Ventriculo-Radial Syndrome
|
Hos1
|
|
Heart Hand Syndrome
|
Atrio Digital Syndrome
|
|
Hos 1
|
Atriodigital Dysplasia Type 1
|
|
Heart-Hand Syndrome Type 1
|
Holt Oram Syndrome
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Congenital Hypothyroidism |
|
Cretinism
|
Neonatal Hypothyroidism
|
|
Ch
|
Cht
|
|
Congenital Myxedema
|
Myxedema, Congenital
|
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
|
| Atrioventricular Septal Defect |
|
AVSD
|
Atrioventricular Canal Defect
|
|
Avcd
|
Endocardial Cushion Defect
|
|
Ecd
|
Avc Defect
|
|
Atrioventricular Septal Defect, Susceptibility To, 1
|
Atrioventricular Septal Defect 1
|
|
Endocardial Cushion Defects
|
Septal Defect, Atrioventricular
|
|
Atrioventricular Defect With Atrial Shunting Only
|
Incomplete Atrioventricular Septal Defect With Isolated Atrial Component
|
|
Incomplete Atrioventricular Canal Defect With Isolated Atrial Component
|
Primum Atrial Septal Defect
|
|
Partial Atrioventricular Canal Defect With Isolated Atrial Component
|
Partial Atrioventricular Septal Defect, Ostium Primum Type
|
|
Ostium Primum Atrial Septal Defect
|
Partial Atrioventricular Canal Defect
|
|
Partial Atrioventricular Septal Defect
|
Atrial Septum Primum Defect
|
|
Atrioventricular Canal Defect With Isolated Ventricular Component
|
Atrioventricular Canal Defect With Isolated Ventricular Communication
|
|
Atrioventricular Septal Defect With Isolated Ventricular Component
|
Atrioventricular Septal Defect With Atrial Shunting And Restrictive Ventricular Shunting
|
|
Intermediate Atrioventricular Canal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valve
|
Transitional Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valves
|
|
Atrioventricular Canal Defect Associated With A Restrictive Ventricular Septal Defect
|
Intermediate Atrioventricular Canal Defect
|
|
Intermediate Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valvar Orifices
|
Intermediate Atrioventricular Septal Defect
|
|
Transitional Atrioventricular Canal Defect
|
Transitional Atrioventricular Septal Defect
|
|
Complete Atrioventricular Canal With Atrial And Ventricular Components
|
Complete Atrioventricular Canal Defect
|
|
Complete Atrioventricular Septal Defect
|
|
|
| Pyloric Stenosis |
|
|
| Ciliary Dyskinesia, Primary, 40 |
|
CILD40
|
Ciliary Dyskinesia, Primary, 40, With Or Without Situs Inversus
|
|
Primary Ciliary Dyskinesia 40
|
Primary Ciliary Dyskinesia 40 With Or Without Situs Inversus
|
|
|
| Syndromic X-Linked Intellectual Disability 34 |
|
Macrocephaly-Intellectual Disability-Left Ventricular Non Compaction Syndrome
|
Mental Retardation, X-Linked, Syndromic 34
|
|
Mrxs34
|
Mrxsml
|
|
Syndromic X-Linked Mental Retardation Mircsof-Langouet Type
|
|
|
| Wolff-Parkinson-White Syndrome |
|
Wolff-Parkinson-White Pattern
|
Wpw Syndrome
|
|
Anomalous Atrioventricular Excitation
|
Anomalous A-V Excitation
|
|
Ventricular Pre-Excitation With Arrhythmia
|
WPWS
|
|
Ventricular Familial Preexcitation Syndrome
|
Preexcitation Syndrome
|
|
Ventricular Preexcitation
|
Wpw - [Wolff-Parkinson- White] Syndrome
|
|
Pre-Excitation Syndrome
|
|
|
| Hypoplastic Right Heart Syndrome |
|
Right Hypoplastic Heart Syndrome
|
|
|
| Tricuspid Atresia |
|
Congenital Agenesis Of The Tricuspid Valve
|
|
|
| Hypertrophic Pyloric Stenosis |
|
Congenital Hypertrophic Pyloric Stenosis
|
Pyloric Stenosis, Hypertrophic
|
|
Congenital Or Infantile Stricture Of Pylorus
|
Achalasia Of The Pylorus
|
|
Congenital Hypertrophy Of The Pylorus
|
Infantile Hypertrophy Of The Pylorus
|
|
Infantile Constriction Of The Pylorus
|
Congenital Stenosis Of The Pylorus
|
|
Congenital Constriction Of The Pylorus
|
Congenital Stricture Of The Pylorus
|
|
Infantile Hypertrophic Pyloric Stenosis
|
Infantile Stenosis Of The Pylorus
|
|
Infantile Stricture Of The Pylorus
|
Congenital Or Infantile Constriction Of Pylorus
|
|
Infantile Pyloric Obstruction
|
Infantile Pyloric Hypertrophy
|
|
Pylorus Achalasia
|
Pyloric Constriction
|
|
Infantile Pyloric Stricture
|
Infantile Pyloric Stenosis
|
|
Congenital Spasm Of Pylorus
|
Congenital Pylorospasm
|
|
Congenital Pyloric Stricture
|
Congenital Pyloric Spasm
|
|
Congenital Or Infantile Spasm Of Pylorus
|
Congenital Or Infantile Obstruction Of Pylorus
|
|
Congenital Pyloric Stenosis
|
|
|
| Tricuspid Valve Disease |
|
Rheumatic Tricuspid Valve Disease
|
Disease Of Tricuspid Valve
|
|
Rh. Tricuspid Valve Disease
|
Rheumatic Disease Of Tricuspid Valve
|
|
Tricuspid Disease
|
Tricuspid Valve Disorder
|
|
|
| Thyroid Malformation |
|
|
| Total Anomalous Pulmonary Venous Return 1 |
|
Scimitar Syndrome
|
Total Anomalous Pulmonary Venous Return
|
|
Anomalous Pulmonary Venous Return
|
Scimitar Anomaly
|
|
TAPVR1
|
Apvr
|
|
Halasz Syndrome
|
Hypogenetic Lung Syndrome
|
|
Pulmonary Venolobar Syndrome
|
TAPVR
|
|
Congenital Total Pulmonary Venous Return Anomaly
|
Congenital Venolobar Syndrome
|
|
Mirror-Image Lung Syndrome
|
Vena Cava Bronchovascular Syndrome
|
|
Pulmonary Venous Return Anomaly
|
Congenital Pulmonary Venolobar Syndrome
|
|
Epibronchial Right Pulmonary Vein Syndrome
|
|
|
| Ovarian Endodermal Sinus Tumor |
|
Endodermal Sinus Tumor Of Ovary
|
Ovarian Yolk Sac Tumor
|
|
Endodermal Sinus Tumour Of Ovary
|
Ovarian Endodermal Sinus Tumour
|
|
Ovarian Yolk Sac Tumour
|
|
|
| Physical Disorder |
|
|
| Myasthenic Syndrome, Congenital, 20, Presynaptic |
|
Congenital Myasthenic Syndrome 20
|
CMS20
|
|
Congenital Myasthenic Syndrome 20 Presynaptic
|
Myasthenic Syndrome, Congenital, Type 20, Presynaptic
|
|
|
| Patent Ductus Arteriosus 1 |
|
Patent Ductus Arteriosus
|
PDA1
|
|
Pda
|
Ductus Arteriosus, Patent
|
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
| Jacobsen Syndrome |
|
Chromosome 11q Deletion Syndrome
|
Partial 11q Monosomy Syndrome
|
|
Jacobsen Distal 11q Deletion Syndrome
|
JBS
|
|
11q Partial Monosomy Syndrome
|
Chromosome 11q Deletion
|
|
11q Deletion
|
11q Monosomy
|
|
Deletion 11q
|
Monosomy 11q
|
|
Partial Monosomy 11q
|
11q Deletion Disorder
|
|
11q Deletion Syndrome
|
11q Terminal Deletion Disorder
|
|
11q- Deletion Syndrome
|
11q23 Deletion Disorder
|
|
Jacobsen Thrombocytopenia
|
11q Terminal Deletion Syndrome
|
|
Del(11)(Q23.3)
|
Del(11)(Qter)
|
|
Distal Deletion 11q
|
Distal Monosomy 11q
|
|
Monosomy 11qter
|
Telomeric Deletion 11q
|
|
Paris-Trousseau Thrombocytopenia
|
|
|
| Ovarian Primitive Germ Cell Tumor |
|
|
| Myasthenic Syndrome, Congenital, 15 |
|
Congenital Myasthenic Syndrome 15
|
CMS15
|
|
Myasthenic Syndrome, Congenital, Without Tubular Aggregates
|
Cmswta
|
|
Myasthenic Syndrome, Congenital, 15, Without Tubular Aggregates
|
Congenital Myasthenic Syndrome 15 Without Tubular Aggregates
|
|
Myasthenic Syndrome, Congenital, Type 15, Without Tubular Aggregates
|
|
|
| Pulmonary Valve Disease |
|
|
| Pulmonary Valve Stenosis |
|
Valvular Pulmonary Stenosis
|
Heart Valve Pulmonary Stenosis
|
|
Valvar Pulmonary Stenosis
|
Valvate Pulmonary Stenosis
|
|
Pulmonary Stenosis
|
Pulmonary Valve Stricture
|
|
Pulmonic Valve Stenosis
|
Ps - [Pulmonary Valve Stenosis]
|
|
Pvs - [Pulmonary Valve Stenosis]
|
Pulmonary Valvular Stricture
|
|
Pulmonary Valvular Stenosis
|
Pulmonary Valvular Obstruction
|
|
Pulmonary Valve Obstruction
|
Obstructed Pulmonary Valve
|
|
|
| Pulmonary Hypertension |
|
Primary Pulmonary Hypertension
|
Hypertension Pulmonary
|
|
Hypertension, Pulmonary
|
Hypertension, Pulmonary, Primary
|
|
Idiopathic Pulmonary Hypertension
|
Idiopathic Pulmonary Arterial Hypertension
|
|
Pulmonary Htn - [Hypertension]
|
|
|
| Transposition Of The Great Arteries, Dextro-Looped |
|
Transposition Of The Great Arteries
|
DTGA1
|
|
Dextro-Looped Transposition Of The Great Arteries
|
DTGA
|
|
Congenitally Uncorrected Transposition Of The Great Arteries
|
Congenitally Uncorrected Transposition Of The Great Vessels
|
|
D-Tga
|
Isolated Ventriculoarterial Discordance
|
|
Ventriculoarterial Discordance With Atrioventricular Concordance
|
Dextro-Transposition Of The Great Arteries
|
|
Transposition Of The Great Vessels
|
Great Vessels Transposition
|
|
Transposition Of The Great Arteries, Dextro-Looped 1
|
Arteries, Great, Transposition, Dextro-Looped
|
|
Ventriculoarterial Discordance, Isolated
|
D-Transposition Of The Great Arteries
|
|
Complete Transposition
|
Tga
|
|
Tgv
|
Transposition Of Great Vessels
|
|
Transposition Of The Great Arteries Dextro-Looped 1
|
Dextro-Looped Transposition Of The Great Arteries 1
|
|
Discordant Ventriculoarterial Connection
|
Complete Transposition Of Great Vessels
|
|
Great Vessels Complete Transposition
|
Total Great Vessel Transposition
|
|
Transposition Of Great Arteries
|
Complete Tga - [Transposition Of The Great Arteries]
|
|
Tga - [Transposition Of Great Arteries]
|
Tgv - [Transposition Of Great Vessels]
|
|
Transposition Of Great Vessels Nos
|
Transposed Vessels Nos
|
|
|
| Atrial Septal Defect 5 |
|
ASD5
|
Atrial Heart Septal Defect 5
|
|
Septal Defect, Atrial, Type 5
|
|
|
| Subvalvular Aortic Stenosis |
|
Fixed Subaortic Stenosis
|
Subaortic Stenosis
|
|
Aortic Stenosis, Subvalvular
|
|
|
| Atrial Septal Defect 2 |
|
ASD2
|
Atrial Heart Septal Defect 2
|
|
Atrial Septal Defect-2
|
Asd Ii
|
|
Septal Defect, Atrial, Type 2
|
|
|
| Patau Syndrome |
|
Trisomy 13
|
Complete Trisomy 13 Syndrome
|
|
Trisomy 13 Syndrome
|
D1 Trisomy
|
|
Patau'S Syndrome
|
Complete Trisomy 13
|
|
Chromosome 13, Trisomy 13 Complete
|
D Trisomy Syndrome
|
|
Bartholin-Patau Syndrome
|
Chromosome 13 Duplication
|
|
D1 Trisomy Syndrome
|
D>1< Trisomy Syndrome
|
|
Patau
|
Chromosome 13 Trisomy
|
|
Abnormal Autosomes 13
|
|
|
| Sinoatrial Node Disease |
|
Sa Node
|
Sinuatrial Node
|
|
Sinus Node Dysfunction
|
|
|
| Ulnar-Mammary Syndrome |
|
Schinzel Syndrome
|
UMS
|
|
Pallister Ulnar-Mammary Syndrome
|
Ulnar-Mammary Syndrome Of Pallister
|
|
|
| Tricuspid Valve Stenosis |
|
Tricuspid Stenosis
|
Tricuspid Stricture
|
|
Tricuspid Valve Stricture
|
Tricuspid Insufficiency With Obstruction
|
|
Tricuspid Insufficiency With Stenosis
|
|
|
| Right Atrial Isomerism |
|
Ivemark Syndrome
|
Asplenia With Cardiovascular Anomalies
|
|
RAI
|
Asplenia Syndrome
|
|
Asplenia
|
Right Isomerism
|
|
Splenic Agenesis Syndrome
|
Bilateral Right-Sidedness Sequence
|
|
Right Sided Atrial Isomerism
|
Isomerism Of Right Atrial Appendage
|
|
Heterotaxy, Visceroatrial, Autosomal Recessive
|
Polyasplenia
|
|
Vah, Autosomal Recessive
|
Atrial Isomerism, Right
|
|
Congenital Absence Of Spleen
|
Bilateral Right-Sidedness
|
|
|
| Orofaciodigital Syndrome Viii |
|
Edwards Syndrome
|
Trisomy 18
|
|
Complete Trisomy 18 Syndrome
|
OFD8
|
|
Orofaciodigital Syndrome 8
|
Trisomy 18 Syndrome
|
|
Oral-Facial-Digital Syndrome With Hypoplastic Epiglottis
|
E3 Trisomy
|
|
Oral-Facial-Digital Syndrome Type 8
|
Orofaciodigital Syndrome Type 8
|
|
Ofds Viii
|
Oral-Facial-Digital Syndrome, Type Viii
|
|
Ofd Syndrome 8
|
Ofds 8
|
|
Oral Facial Digital Syndrome 8
|
Oral Facial Digital Syndrome Type 8
|
|
18 Trisomy
|
Chromosome 18 Trisomy
|
|
Trisomy 16-18
|
Trisomy E
|
|
Trisomy E Syndrome
|
Chromosome 18 Duplication
|
|
Oral-Facial-Digital Syndrome, Edwards Type
|
Orofaciodigital Syndrome, Edwards Type
|
|
Chromosome 18, Trisomy
|
Cleft Lip/Palate With Abnormal Thumbs And Microcephaly
|
|
Trisomy 18 Chromosome
|
Abnormal Autosomes 18
|
|
|
| Fanconi Renotubular Syndrome 1 |
|
Renal Fanconi Syndrome
|
Adult Fanconi Syndrome
|
|
FRTS1
|
Fanconi Renotubular Syndrome
|
|
Frts
|
Rfs
|
|
Fanconi Syndrome Without Cystinosis
|
Luder-Sheldon Syndrome
|
|
|
| Pulmonary Valve Insufficiency |
|
Pulmonary Regurgitation
|
Pulmonary Incompetence
|
|
Pulmonary Incompetence, Non-Rheumatic
|
Pulmonary Insufficiency Following Trauma And Surgery
|
|
Pulmonary Regurg.
|
Pulmonic Insufficiency
|
|
Pulmonic Valve Regurgitation
|
Pulmonary Valve Incompetence
|
|
Pulmonary Valve Incompetency
|
Pulmonary Valvular Insufficiency
|
|
Pulmonary Valvular Regurgitation
|
Pulmonary Valvular Incompetency
|
|
Pulmonary Valve Incompetence Nos
|
Annular Incompetency Pulmonary Valve
|
|
Incompetent Pulmonary Valve
|
Graham Steell Murmur
|
|
Pulmonary Valvular Incompetence
|
|
|
| Endocardial Fibroelastosis |
|
Endomyocardial Fibroelastosis
|
Elastomyofibrosis
|
|
EFE
|
Efe - [Endocardial Fibroelastosis]
|
|
Primary Endocardial Fibroelastosis
|
Fibroelastosis Cordis
|
|
Fetal Endocarditis
|
Fibroelastosis
|
|
Congenital Endocardial Fibroelastosis
|
Congenital Valvular Endocarditis
|
|
|
| Germ Cell And Embryonal Cancer |
|
Germ Cell And Embryonal Neoplasm
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Aortic Valve Insufficiency |
|
Aortic Regurgitation
|
Rheumatic Aortic Regurgitation
|
|
Aortic Insufficiency
|
Rheumatic Aortic Insufficiency
|
|
Rheumatic Aortic Valve Insufficiency
|
Aortic Incompetence
|
|
Corrigan'S Disease
|
Rheumatic Aortic Valve Regurgitation
|
|
Aortic Valve Incompetency
|
Ai - [Aortic Incompetence]
|
|
Incompetent Aortic Valve
|
Ar - [Aortic Regurgitation]
|
|
Calcific Aortic Valve Regurgitation
|
Myxomatous Aortic Valve Regurgitation
|
|
Annular Incompetency Of Aortic Valve
|
Austin Flint Murmur
|
|
Flint Murmur
|
Rheumatic Aortic Incompetence
|
|
Rheumatic Ai - [Aortic Insufficiency]
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| Chromosomal Deletion Syndrome |
|
|
| Germ Cell Cancer |
|
Malignant Germ Cell Tumor
|
Neoplasms, Germ Cell And Embryonal
|
|
Germ Cell Neoplasm
|
Germ Cell Tumour
|
|
Malignant Tumor Of The Germ Cell
|
Neoplasms Germ Cell
|
|
Malignant Germ Cell Neoplasm
|
|
|
| Wolf-Hirschhorn Syndrome |
|
Pitt-Rogers-Danks Syndrome
|
WHS
|
|
Chromosome 4p16.3 Deletion Syndrome
|
Wittwer Syndrome
|
|
4p- Syndrome
|
Pitt Syndrome
|
|
4p Deletion Syndrome
|
Distal Deletion 4p
|
|
Distal Monosomy 4p
|
Telomeric Deletion 4p
|
|
Prds
|
4p Syndrome
|
|
Chromosome 4p Syndrome
|
Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation
|
|
Wolf Syndrome
|
Chromosome 4p Deletion Syndrome
|
|
Chromosome 4p Monosomy
|
Del Syndrome
|
|
Monosomy 4p
|
Partial Monosomy 4p
|
|
Chromosome 4 Short Arm Deletion
|
|
|
| Axenfeld-Rieger Syndrome |
|
Axenfeld Syndrome
|
Rieger Syndrome
|
|
Rieger Anomaly
|
Axenfeld Anomaly
|
|
Anomaly, Rieger'S
|
Hagedoom Syndrome
|
|
Rgs - Rieger Syndrome
|
Rieger'S Anomaly
|
|
Goniodysgenesis Hypodontia
|
Iridogoniodysgenesis With Somatic Anomalies
|
|
Ars
|
Axenfeld And Rieger Anomaly
|
|
Axra
|
Axrs
|
|
Rieger Eye Malformation Sequence
|
|
|
| Noonan Syndrome With Multiple Lentigines |
|
Leopard Syndrome
|
Multiple Lentigines Syndrome
|
|
Moynahan Syndrome
|
Cardiomyopathic Lentiginosis
|
|
Progressive Cardiomyopathic Lentiginosis
|
Cardio-Cutaneous Syndrome
|
|
Lentiginosis Profusa
|
Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome
|
|
Generalized Lentiginosis
|
Gorlin Syndrome Ii
|
|
Lentiginosis Profusa Syndrome
|
Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes
|
|
Diffuse Lentiginosis
|
Nsml
|
|
Familial Multiple Lentigines Syndrome
|
Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type
|
|
Progressive Cardiomyopathic Lentiginosis Syndrome
|
Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Aortic Valve Disease 2 |
|
Aortic Valve Stenosis
|
Aortic Stenosis
|
|
Rheumatic Aortic Stenosis
|
AOVD2
|
|
Bicuspid Aortic Valve
|
Rheumatic Aortic Valve Stenosis
|
|
Valvular Aortic Stenosis
|
Aortic Valve Disease, Type 2
|
|
Aortic Valve Stricture
|
Aortic Valve Obstruction
|
|
Obstructed Aorta Valve
|
Rheumatic Aortic Obstruction
|
|
Rheumatic Aortic Valve Obstruction
|
Rheumatic Aortic Stricture
|
|
Aortic Valve Regurgitation
|
Aortic Insufficiency With Stenosis
|
|
Rheumatic Aortic Valve Stenosis With Insufficiency
|
Rheumatic Aortic Stenosis With Incompetence
|
|
Rheumatic Aortic Stenosis With Regurgitation
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Velocardiofacial Syndrome |
|
Shprintzen Syndrome
|
VCFS
|
|
Chromosome 22q11.2 Deletion Syndrome
|
Vcf Syndrome
|
|
Shprintzen Vcf Syndrome
|
Vcf-Velocardiofacial Syndrome
|
|
Velo-Cardio-Facial Syndrome
|
Digeorge Syndrome
|
|
22q11 Deletion Syndrome
|
Conotruncal Anomaly Face Syndrome
|
|
|
| Chromosome 1p36 Deletion Syndrome |
|
1p36 Deletion Syndrome
|
Deletion 1p36
|
|
Monosomy 1p36
|
Subtelomeric 1p36 Deletion
|
|
Monosomy 1p36 Syndrome
|
Distal Monosomy 1p36
|
|
Del(1)(P36)
|
Deletion 1pter
|
|
Monosomy 1pter
|
|
|
| Chromosome 22q11.2 Deletion Syndrome, Distal |
|
22q11.2 Deletion Syndrome
|
Autosomal Dominant Opitz G/Bbb Syndrome
|
|
Catch22
|
Cayler Cardiofacial Syndrome
|
|
Conotruncal Anomaly Face Syndrome
|
Digeorge Syndrome
|
|
Sedlackova Syndrome
|
Shprintzen Syndrome
|
|
Velocardiofacial Syndrome
|
22q11.2 Distal Deletion Syndrome
|
|
Distal 22q11.2 Microdeletion Syndrome
|
22q11.2ds
|
|
Vcfs
|
Velo-Cardio-Facial Syndrome
|
|
Distal Chromosome 22q11.2 Deletion Syndrome
|
Chromosome 22q11.2 Deletion Syndrome Distal
|
|
Chromosome 22q11.2 Deletion Syndrome
|
Deletion 22q11.2 Syndrome
|
|
22q11ds
|
Catch 22
|
|
Digeorge Sequence
|
Microdeletion 22q11.2
|
|
Monosomy 22q11
|
Takao Syndrome
|
|
Distal Del(22)(Q11.2)
|
Distal Monosomy 22q11.2
|
|
Catch 22 Syndrome
|
Chromosome Deletion Syndrome 22q11.2, Distal
|
|
|
| Kabuki Syndrome 1 |
|
Kabuki Syndrome
|
Niikawa-Kuroki Syndrome
|
|
Kabuki Make-Up Syndrome
|
Kms
|
|
KABUK1
|
Kabuki Make Up Syndrome
|
|
Nks
|
Kabuki Makeup Syndrome
|
|
Kabuki Syndrome, Type 1
|
|
|
| Brugada Syndrome |
|
Sudden Unexpected Nocturnal Death Syndrome
|
Sudden Unexplained Nocturnal Death Syndrome
|
|
Bangungut
|
Brugada Type Idiopathic Ventricular Fibrillation
|
|
Pokkuri Death Syndrome
|
Sunds
|
|
Idiopathic Ventricular Fibrillation, Brugada Type
|
Sudden Unexplained Death
|
|
Dream Disease
|
Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
|
|
Sudden Unexplained Death Syndrome
|
Suds
|
|
Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
|
|
|
| Orthostatic Intolerance |
|
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
|
Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
|
Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
|
OI
|
Intolerance, Orthostatic
|
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
|
Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Aortic Aneurysm, Familial Thoracic 1 |
|
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
|
AAT1
|
Faa1
|
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
|
Aneurysm, Thoracic Aortic
|
Faa
|
|
Ftaad
|
Taa
|
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
|
Dissection Of Thoracic Aorta
|
|
|
| Long Qt Syndrome 1 |
|
Romano-Ward Syndrome
|
LQT1
|
|
Ward-Romano Syndrome
|
Rws
|
|
Ventricular Fibrillation With Prolonged Qt Interval
|
Wrs
|
|
Long Qt Syndrome 1, Acquired, Susceptibility To
|
Long Qt Syndrome 1, Acquired
|
|
Romano-Ward Long Qt Syndrome
|
Long Qt Syndrome Type 1
|
|
Long Qt Syndrome-1
|
Acquired Susceptibility To Long Qt Syndrome 1
|
|
Qt Syndrome, Long, Type 1
|
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Cardiomyopathy, Hypertrophic, Familial
|
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 1 |
|
Asymmetric Septal Hypertrophy
|
Familial Hypertrophic Cardiomyopathy
|
|
Hypertrophic Cardiomyopathy 1
|
CMH1
|
|
Hypertrophic Cardiomyopathy 19
|
CMH
|
|
Ventricular Hypertrophy, Hereditary
|
Ash
|
|
Hypertrophic Subaortic Stenosis, Idiopathic
|
Cardiomyopathy, Familial Hypertrophic
|
|
Cardiomyopathy, Hypertrophic, 1, Digenic
|
Cardiomyopathy, Familial Hypertrophic 1
|
|
Hcm
|
Hereditary Ventricular Hypertrophy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Hypertrophic Cardiomyopathy
|
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiomyopathy, Hypertrophic, 1
|
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
|
Fhc
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
|
| Visceral Heterotaxy |
|
Situs Ambiguus
|
Heterotaxia
|
|
Heterotaxy Syndrome
|
Heterotaxy
|
|
Lateralization Defect
|
Situs Ambiguous
|
|
Left Isomerism
|
Htx
|
|
Ivemark Syndrome
|
Right Isomerism
|
|
Situs Ambiguus Viscerum
|
Incomplete Situs Inversus
|
|
Partial Situs Inversus
|
Heterotaxy, Visceral
|
|
Asplenia Syndrome
|
Bilateral Left-Sidedness
|
|
Polysplenia Syndrome
|
Moller Syndrome
|
|
|
| Williams-Beuren Syndrome |
|
Williams Syndrome
|
WBS
|
|
Wms
|
Deletion 7q11.23
|
|
Monosomy 7q11.23
|
Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb
|
|
Fanconi Schlesinger Syndrome
|
Beuren Syndrome
|
|
Elfin Facies Syndrome
|
Elfin Facies With Hypercalcemia
|
|
Hypercalcemia-Supravalvar Aortic Stenosis
|
Ws
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
